Stent, Ureteral
Gyrus Acmi, Inc.'s record for this product code
MDR events13All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
13 adverse event reports on file
- URO-GUIDE,6.0 X 22 CM WO/GWOct 10, 2024Malfunction3011050570-2024-00424
- URO-GUIDE 6.0X 28Oct 10, 2024Malfunction3011050570-2024-00425
- URO-GUIDE 6.0X24 CM W/O WIREOct 10, 2024Malfunction3011050570-2024-00423
- URO-GUIDE 8.5 X 26 CM WO/ GWSep 29, 2024Injury3011050570-2024-00393
- URO-GUIDE 8.5 X 26 CM WO/ GWSep 29, 2024Injury3011050570-2024-00394
- URO-GUIDE 8.5 X 26 CM WO/ GWSep 29, 2024Injury3011050570-2024-00395
- URO-GUIDE 8.5 X 26 CM WO/ GWSep 29, 2024Injury3011050570-2024-00396
- URO GUIDE 6 FR X 26 CMSep 23, 2024Injury3011050570-2024-00385
- LITHOSTENT 7.0X28CMJan 1, 2024Malfunction3011050570-2024-00003
- SOF-CURL URETERAL STENT 6.0X24Nov 21, 2023Injury3003790304-2023-00434
Recalls
0 recall events for this product code
No recalls on file for Gyrus Acmi, Inc. under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Gyrus Acmi, Inc. under this product code.